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Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer
Altered platelet indices, including platelet count (PC), mean platelet volume (MPV), platelet distribution width (PDW), and plateletcrit (PCT), have been found in various cancer types. This study aimed to evaluate the role of platelet indices as potential biomarkers for the diagnosis of colorectal c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081379/ https://www.ncbi.nlm.nih.gov/pubmed/30087357 http://dx.doi.org/10.1038/s41598-018-29293-x |
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author | Zhu, Xianjin Cao, Yingping Lu, Pingxia Kang, Yanli Lin, Zhen Hao, Taisen Song, Yanfang |
author_facet | Zhu, Xianjin Cao, Yingping Lu, Pingxia Kang, Yanli Lin, Zhen Hao, Taisen Song, Yanfang |
author_sort | Zhu, Xianjin |
collection | PubMed |
description | Altered platelet indices, including platelet count (PC), mean platelet volume (MPV), platelet distribution width (PDW), and plateletcrit (PCT), have been found in various cancer types. This study aimed to evaluate the role of platelet indices as potential biomarkers for the diagnosis of colorectal cancer (CRC), and to assess the association between platelet indices and CRC clinicopathological characteristics. The study included 783 subjects with CRC, 463 subjects with colorectal adenomas (CA), and 689 control subjects from June 2015 to October 2017. All participants’ clinicopathological characteristics were collected and analyzed. Here, we found that PC, MPV and PCT levels in CRC patients were significantly higher than those in CA patients and healthy participants (p < 0.001); however, PDW level in CRC patients was significantly higher than that in healthy participants while lower than that in CA patients. Receiver-operating characteristic (ROC) analysis indicated that combined detection of PCT and CEA appears to be a more effective marker to distinguish CRC patients from CA patients, with 70% sensitivity and 83% specificity. Among CRC patients, PC and PCT levels were associated with TNM stages and tumor size; MPV and PCT levels were associated with vascular invasion. Our findings suggest that altered PC, MPV and PCT levels might serve as potential biomarkers for the diagnosis and prognosis of CRC. |
format | Online Article Text |
id | pubmed-6081379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60813792018-08-10 Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer Zhu, Xianjin Cao, Yingping Lu, Pingxia Kang, Yanli Lin, Zhen Hao, Taisen Song, Yanfang Sci Rep Article Altered platelet indices, including platelet count (PC), mean platelet volume (MPV), platelet distribution width (PDW), and plateletcrit (PCT), have been found in various cancer types. This study aimed to evaluate the role of platelet indices as potential biomarkers for the diagnosis of colorectal cancer (CRC), and to assess the association between platelet indices and CRC clinicopathological characteristics. The study included 783 subjects with CRC, 463 subjects with colorectal adenomas (CA), and 689 control subjects from June 2015 to October 2017. All participants’ clinicopathological characteristics were collected and analyzed. Here, we found that PC, MPV and PCT levels in CRC patients were significantly higher than those in CA patients and healthy participants (p < 0.001); however, PDW level in CRC patients was significantly higher than that in healthy participants while lower than that in CA patients. Receiver-operating characteristic (ROC) analysis indicated that combined detection of PCT and CEA appears to be a more effective marker to distinguish CRC patients from CA patients, with 70% sensitivity and 83% specificity. Among CRC patients, PC and PCT levels were associated with TNM stages and tumor size; MPV and PCT levels were associated with vascular invasion. Our findings suggest that altered PC, MPV and PCT levels might serve as potential biomarkers for the diagnosis and prognosis of CRC. Nature Publishing Group UK 2018-08-07 /pmc/articles/PMC6081379/ /pubmed/30087357 http://dx.doi.org/10.1038/s41598-018-29293-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhu, Xianjin Cao, Yingping Lu, Pingxia Kang, Yanli Lin, Zhen Hao, Taisen Song, Yanfang Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title | Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title_full | Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title_fullStr | Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title_full_unstemmed | Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title_short | Evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
title_sort | evaluation of platelet indices as diagnostic biomarkers for colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081379/ https://www.ncbi.nlm.nih.gov/pubmed/30087357 http://dx.doi.org/10.1038/s41598-018-29293-x |
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